βNever again.β That was what she said when she left. She promised herself she would never live that life, never return to all that pain. There was nothing in the world that could make her go back β¦ or so she thought. For a while she kept that promise, and she was finally happy. She built a life f
Inherited macrocephaly-hamartoma syndromes
β Scribed by DiLiberti, John H.
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 19 KB
- Volume
- 79
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(19981002)79:4<284::aid-ajmg10>3.0.co;2-n
No coin nor oath required. For personal study only.
β¦ Synopsis
Recent discoveries in the molecular biology of the phosphatase and tensin homolog (PTEN) locus in the q22-23 region of chromosome 10 prove and/or suggest that several syndromes previously considered to be clinically and genetically distinct entities should actually be unified into a single entity. This conclusion is most secure for the Cowden and ''Bannayan-Zonana'' phenotypes, but almost certainly should also include the ''Riley-Ruvalcaba'' and Lhermitte-Duclos phenotypes as well benign familial macrocephaly and external hydrocephalus. The clinical and molecular data supporting this unification are presented along with a proposal for new nomenclature-the PTEN MATCHS (macrocephaly, autosomal dominant, thyroid disease, cancer, hamartomata, skin abnormalities) syndrome-based on the observed clinical abnormalities.
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